PanelApp
  1. Genes and Genomic Entities
  2. CHCHD2

CHCHD2

coiled-coil-helix-coiled-coil-helix domain containing 2
OMIM: 616244, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green CHCHD2 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.43

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions
  • Tremors_Superpanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Parkinson disease 22, autosomal dominant MIM#616710

    Green CHCHD2 in Incidentalome


    Version 0.360

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Parkinson disease 22, autosomal dominant MIM#616710
    Tags
    • adult onset neurodegenerative

    Green CHCHD2 in Mitochondrial disease


    Level 2: Metabolic disorders
    Version 0.1085

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Parkinson disease 22, autosomal dominant MIM#616710